CN1216901C - 使用加工酶的嵌合蛋白质的切断方法 - Google Patents

使用加工酶的嵌合蛋白质的切断方法 Download PDF

Info

Publication number
CN1216901C
CN1216901C CN971096937A CN97109693A CN1216901C CN 1216901 C CN1216901 C CN 1216901C CN 971096937 A CN971096937 A CN 971096937A CN 97109693 A CN97109693 A CN 97109693A CN 1216901 C CN1216901 C CN 1216901C
Authority
CN
China
Prior art keywords
sequence
chimeric protein
arg
peptide
kex2
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN971096937A
Other languages
English (en)
Chinese (zh)
Other versions
CN1167155A (zh
Inventor
铃木雄司
孙田浩二
增田丰文
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sankyo Co Ltd
Original Assignee
Daiichi Suntory Pharma Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daiichi Suntory Pharma Co Ltd filed Critical Daiichi Suntory Pharma Co Ltd
Publication of CN1167155A publication Critical patent/CN1167155A/zh
Application granted granted Critical
Publication of CN1216901C publication Critical patent/CN1216901C/zh
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04Linear peptides containing only normal peptide links
    • C07K7/06Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575Hormones
    • C07K14/585Calcitonins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/12General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by hydrolysis, i.e. solvolysis in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575Hormones
    • C07K14/635Parathyroid hormone, i.e. parathormone; Parathyroid hormone-related peptides
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/62DNA sequences coding for fusion proteins
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/24Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2468Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1) acting on beta-galactose-glycoside bonds, e.g. carrageenases (3.2.1.83; 3.2.1.157); beta-agarase (3.2.1.81)
    • C12N9/2471Beta-galactosidase (3.2.1.23), i.e. exo-(1-->4)-beta-D-galactanase
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y302/00Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01023Beta-galactosidase (3.2.1.23), i.e. exo-(1-->4)-beta-D-galactanase
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/50Fusion polypeptide containing protease site
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/70Fusion polypeptide containing domain for protein-protein interaction
    • C07K2319/74Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor
    • C07K2319/75Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor containing a fusion for activation of a cell surface receptor, e.g. thrombopoeitin, NPY and other peptide hormones

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Biomedical Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Endocrinology (AREA)
  • Microbiology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Toxicology (AREA)
  • Physics & Mathematics (AREA)
  • Plant Pathology (AREA)
  • Analytical Chemistry (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Saccharide Compounds (AREA)
CN971096937A 1996-03-04 1997-03-04 使用加工酶的嵌合蛋白质的切断方法 Expired - Fee Related CN1216901C (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP70906/96 1996-03-04
JP70906/1996 1996-03-04
JP7090696 1996-03-04

Publications (2)

Publication Number Publication Date
CN1167155A CN1167155A (zh) 1997-12-10
CN1216901C true CN1216901C (zh) 2005-08-31

Family

ID=13445041

Family Applications (1)

Application Number Title Priority Date Filing Date
CN971096937A Expired - Fee Related CN1216901C (zh) 1996-03-04 1997-03-04 使用加工酶的嵌合蛋白质的切断方法

Country Status (11)

Country Link
US (1) US5891671A (ja)
EP (1) EP0794255B1 (ja)
JP (1) JP3925982B2 (ja)
KR (1) KR100468268B1 (ja)
CN (1) CN1216901C (ja)
AT (1) ATE290088T1 (ja)
AU (1) AU734397B2 (ja)
CA (1) CA2198966C (ja)
DE (1) DE69732583T2 (ja)
DK (1) DK0794255T3 (ja)
TW (1) TW480270B (ja)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2284847A1 (en) * 1998-01-30 1999-08-05 Suntory Limited Process for producing peptides using a helper peptide
CN1170932C (zh) * 1998-07-10 2004-10-13 赛欧斯公司 生产等电点高于8或低于5的多肽的方法
PT1197496E (pt) 1999-07-23 2007-08-29 Kenji Kangawa Novos péptidos
EP1234038A1 (en) * 1999-11-19 2002-08-28 Transkaryotic Therapies, Inc. Nucleic acid construct for optimized production of products
US6730306B1 (en) * 2000-03-08 2004-05-04 Large Scale Biology Corporation Parvovirus vaccine as viral coat protein fusions
CA2472235C (en) 2002-04-11 2012-05-22 Daiichi Suntory Pharma Co., Ltd. A method for producing a modified peptide
GB0308734D0 (en) * 2003-04-15 2003-05-21 Axcess Ltd Uptake of macromolecules
GB0308732D0 (en) * 2003-04-15 2003-05-21 Axcess Ltd Absorption enhancers
JP6817939B2 (ja) 2014-12-01 2021-01-20 フェネックス インク. ペプチド産生のための融合パートナー
CN110305223B (zh) * 2019-06-26 2022-05-13 重庆派金生物科技有限公司 重组串联融合蛋白制备目标多肽的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60217894A (ja) * 1984-04-14 1985-10-31 Suntory Ltd 新規プロテア−ゼ及びその製造方法
RU2091490C1 (ru) * 1985-10-25 1997-09-27 Зимодженетикс, Инк. Способ получения гетерологичного полипептида в эукариотических микроорганизмов
DE3805150A1 (de) * 1987-04-11 1988-10-20 Hoechst Ag Gentechnologisches verfahren zur herstellung von polypeptiden
DE3725320A1 (de) * 1987-07-30 1989-02-09 Biotechnolog Forschung Gmbh Expressionsvektoren und verfahren unter deren verwendung zur gewinnung von cro/ss-galaktosidase/pth-fusionsproteinen und von pth
JPH07108232B2 (ja) * 1990-10-09 1995-11-22 エム・ディ・リサーチ株式会社 ペプチド又は蛋白質の製造方法
JPH05328492A (ja) * 1992-05-21 1993-12-10 Matsushita Electric Ind Co Ltd スピーカ用ダンパー
CA2198968C (en) * 1996-03-04 2010-02-09 Toyofumi Masuda Process for production of secretory kex2 derivatives

Also Published As

Publication number Publication date
AU1503697A (en) 1997-09-11
AU734397B2 (en) 2001-06-14
JPH09296000A (ja) 1997-11-18
EP0794255B1 (en) 2005-03-02
EP0794255A3 (en) 1999-01-27
DE69732583D1 (de) 2005-04-07
EP0794255A2 (en) 1997-09-10
DK0794255T3 (da) 2005-06-27
ATE290088T1 (de) 2005-03-15
CN1167155A (zh) 1997-12-10
KR100468268B1 (ko) 2005-06-27
CA2198966C (en) 2011-06-21
JP3925982B2 (ja) 2007-06-06
CA2198966A1 (en) 1997-09-04
DE69732583T2 (de) 2006-01-19
TW480270B (en) 2002-03-21
KR970065554A (ko) 1997-10-13
US5891671A (en) 1999-04-06

Similar Documents

Publication Publication Date Title
CN1198937C (zh) 利用辅助肽制造肽的方法
CN1231595C (zh) 通过分子伴侣的共分泌制备天然折叠的和分泌的蛋白质的方法
CN1177926C (zh) 产l-谷氨酸棒状细菌及生产l-谷氨酸的方法
CN1115413C (zh) 合成前导肽序列
CN1158305C (zh) 增强了锌结合力的胰岛素衍生物
CN1151252C (zh) 生产微生物转谷氨酰胺酶的方法
CN1216988C (zh) 分泌型Kex衍生物的制造方法
CN1531595A (zh) 琼脂糖酶及其基因
CN1703421A (zh) 降低peg化蛋白的聚集体水平的方法
CN88100146A (zh) 胰蛋白酶抑制剂
CN1216901C (zh) 使用加工酶的嵌合蛋白质的切断方法
CN101074435A (zh) α-半乳糖苷酶基因、其编码蛋白及其制备方法和应用
CN1195859C (zh) 修饰化人源粒细胞-集落刺激因子及其制备方法
CN1152955C (zh) 生产蛋白酶的方法
CN1545553A (zh) 生产重组胰蛋白酶的方法
CN1192037C (zh) 用于由大肠杆菌向培养基中分泌来制备Leu-水蛭素的信号序列
CN1592785A (zh) 酵母中来自Tritirachium album的重组蛋白酶K的表达
CN1178798A (zh) 去除n-末端蛋氨酸的方法
CN1153831C (zh) 编码神经酰胺糖内切酶激活物的基因
CN1154727C (zh) 人甲状旁腺素的重组表达载体
CN1311074C (zh) 重组表达的羧肽酶b及其纯化
CN1250728C (zh) 在原核细胞内产生活性异二聚体amv-rt的方法
CN1948339A (zh) 端粒酶活性抑制蛋白的制备和纯化
CN1181196C (zh) 来自真菌的α-1,4-葡聚糖裂解酶,其纯化,基因克隆和在微生物中的表达
CN1322211A (zh) 除去n-末端蛋氨酸的方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
ASS Succession or assignment of patent right

Owner name: SUNTORY LTD

Free format text: FORMER OWNER: SUNTORY LTD.

Effective date: 20030425

C41 Transfer of patent application or patent right or utility model
TA01 Transfer of patent application right

Effective date of registration: 20030425

Address after: Tokyo, Japan

Applicant after: Daiichi Suntory Pharma Co., Ltd.

Address before: Osaka

Applicant before: Suntory Ltd.

C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee

Owner name: THE FIRST ASHBIAO PHARMACEUTICAL CO., LTD.

Free format text: FORMER NAME OR ADDRESS: SUNTORY LTD

CP03 Change of name, title or address

Address after: Tokyo, Japan

Patentee after: Daiichi Asubio Pharma Co., Ltd.

Address before: Tokyo, Japan

Patentee before: Daiichi Suntory Pharma Co., Ltd.

C56 Change in the name or address of the patentee

Owner name: ASTERIX PHARMACEUTICAL CO., LTD.

Free format text: FORMER NAME OR ADDRESS: THE FIRST ASHBIAO PHARMACEUTICAL CO., LTD.

CP03 Change of name, title or address

Address after: Tokyo, Japan

Patentee after: Asubio Pharma Co., Ltd.

Address before: Tokyo, Japan

Patentee before: Daiichi Asubio Pharma Co., Ltd.

ASS Succession or assignment of patent right

Owner name: SANKYO CO.

Free format text: FORMER OWNER: ASUBIO PHARMA CO., LTD.

Effective date: 20100916

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: JAPAN TOKYO TO: TOKYO, JAPAN

TR01 Transfer of patent right

Effective date of registration: 20100916

Address after: Tokyo, Japan

Patentee after: Sankyo Co.

Address before: Tokyo, Japan

Patentee before: Asubio Pharma Co., Ltd.

C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20050831

Termination date: 20120304